IMI (UDI 08033481792128)
Manufactured by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.
Device Regulatory Overview
The IMI (Model/Catalog Number: TL108CA) is a medical device manufactured by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.. This product is indexed under FDA Product Code / Category Classification A020102020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TL108CA
- Product Code / EMDN
- A020102020101
- Device Name
- Syringe 50/60ml Luer Lock with needle
- Database Sync Date
- 2026-08-09 16:29:09
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of IMI?
The registered manufacturer of record for IMI is I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C..
What is the Primary UDI-DI identifier for IMI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033481792128.
What classification code is assigned to this device?
This device is registered under product classification code A020102020101.
Similar Classification Devices (A020102020101)
Other Devices by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.
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